HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → Ethyl 5-hydroxy-4-nitroindole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Ethyl 5-methoxyindole-2-carboxylate | HCID 20926 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 5-hydroxy-4-nitroindole-2-carboxylate | HCID 22030612 | 59% |
Reaction Steps
A mixture of ethyl 5-methoxyindole-2-carboxylate (8.15 g, 37.2 mmol), (prepared by the method described in Heterocycles Vol. 43, No. 2, p. 263–266), nitric acid adsorbed on silica gel (24 g) and dichloromethane (150 ml) was stirred at ambient temperature for 18 hours. The dichloromethane was removed in vacuo and the product washed off the silica with acetone. The acetone was evaporated in vacuo. The residue was treated again with nitric acid on silica (1 g) as above and the work up procedure repeated to give ethyl 5-hydroxy-4-nitroindole-2-carboxylate (5.8 g, 59%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074800B1 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-c0d5244af2d04652bf6b3bc60250d25d |
| Source note | uspto-grants-2006_07 |